Organophosphate Esters Concentrations Research Articles

Organophosphate esters and synthetic musks in the sediments of the Yangtze River Estuary and adjacent East China Sea: Occurrence, distribution, and potential ecological risks

Occurrence, distribution, and potential ecological risks of ten organophosphate esters (OPEs) and nine synthetic musks (SMs) were investigated in sediments from the Yangtze River Estuary (YRE) and adjacent East China Sea (ECS). The total concentrations of OPEs in the surface sediments ranged from 0.977 to 19.0 ng/g dry weight (dw) with tris(2-chloro-propyl) phosphate being the dominant component. Total concentrations of SMs ranged from 0.176 to 7.25 ng/g dw, with 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta(g)-2-benzopyran and 7-acetyl-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthalene as the dominant SMs. Higher sedimentary concentrations of ΣOPEs and ΣSMs were found in the river mouths of the YRE, inter face of Hangzhou Bay, and mud area of the ECS; the results suggested that terrestrial discharge might be the main source of OPEs and SMs in the studied region. Risk assessment revealed that low ecological risks were posed by OPEs, and limited to low ecological risks were posed by SMs.

Organophosphate esters exposure in relation to glucose homeostasis and type 2 diabetes in adults: A national cross-sectional study from the national health and nutrition survey

BackgroundExposure to organophosphate esters (OPEs) may be associated with impaired glucose homeostasis and increased risk of type 2 diabetes (T2D) in adolescent. However, the evidence in general population is scarce, especially for glucose homeostasis. We used data from the National Health and Nutrition Examination Survey (NHANES) 1999–2008 and 2011–2012 to investigate the relationship of urinary OPEs with glucose homeostasis and T2D in adults. MethodsA total of 5347 participants aged ≥20 years were included. The exposures were the concentrations of urinary OPEs metabolites [dimethyl phosphate (DMP), dimethyl thiophosphate (DMTP), dimethyl dithiophosphate (DMDTP), diethyl phosphate (DEP), diethyl thiophosphate (DETP), and diethyl dithiophosphate (DEDTP)]. The health outcomes were prevalence of T2D and glucose homeostasis [i.e., fasting glucose, 2-h plasma glucose during a 75-g oral glucose tolerance test (2 h-OGTT), serum insulin, HemoglobinA1c (HbA1c), HOMA-IR, and HOMA-β]. The multivariable linear regression model was used to evaluate the relationship between OPEs and glucose homeostasis. The multivariable binary logistic regression analysis was used to investigate the relationship between OPEs and prevalence of T2D. ResultsThe OPEs compound DMTP was significantly associated with higher levels of serum insulin [β (95%confidence interval, CI) = 0.21 (0.06,0.36), for one unit increase in log2-transformed exposure] and HOMA IR [β (95%CI) = 0.08 (0.02,0.14)], and increased odds of T2D [odds ratio (95% CI) = 1.05 (1.01–1.08)]. Other OPEs were not statistically associated with the serum markers for glucose homeostasis or T2D prevalence. ConclusionOur study found that the OPEs compound DMTP might be associated with impaired glucose homeostasis and may increase the prevalence of T2D in U.S. adults. Further longitudinal or experimental studies are warranted to verify our findings in different populations and different OPEs concentrations.

Elevated concentration and high Diversity of organophosphate esters (OPEs) were Discovered in Sediment from Industrial, and E-Waste Recycling Areas

Aquatic environments in industrial, and e-waste recycling areas might undergo severe contamination; however, there are few studies comprehensively assessing the pollution status of organophosphate esters (OPEs) in these two areas. Here, we applied both atmospheric pressure chemical ionization (APCI) and electron spray ionization (ESI) sources in our target, suspect, and functional group-dependent screening strategy, which enhanced the confidence for confirmation on precursor ions of OPEs. Then, n=53 sediment samples (30 from the industrial area, and 23 from the e-waste recycling area) were analyzed. Twenty-three out of 30 target OPEs were quantifiable in these analyzed samples. Total OPE concentrations (Σ30OPEs) in samples from e-waste recycling area range from 12.8 to 9250 ng/g dry weight (dw), that are statistically significantly greater (t-test, p < 0.001) than those from industrial area (25.1-5520 ng/g dw). Σ30OPEs in the sediments from industrial, or e-waste recycling area are statistically significantly greater (one-way ANOVA, p < 0.001) as compared to those (32.0-369 ng/g dw) from Taihu Lake in our previous study. In sediment from three areas, suspect and non-target analysis fully or tentatively identified other 20 OPEs. Four of them have not been recorded or registered in any of online chemical databases, and they are tentatively named as ((methoxy(phenoxy)phosphoryl)oxy)phenyl diphenyl phosphate (mPPODP), (tert-butyl)phenyl (ethyne-oxidane) bis(2,4-di-tert-butylphenyl) phosphate (TPBDTP), bis(dichlorophenyl) propane-1,3-diyl bis(hexylated phosphate) (BDCBHP), and bis(2-hexadecoxyethyl) ethyl phosphate (BHEPP). Overall, this study provided new insights regarding both analytical methodology and pollution status of OPEs, and highlights that elevated concentrations and high diversity of OPEs exist in sediments from industrial, and e-waste recycling areas.

Characterization of organophosphate esters (OPEs) and polyfluoralkyl substances (PFASs) in settled dust in specific workplaces

An analytical method for detecting flame retardants was slightly modified and optimized for the simultaneous determination of 11 organophosphate esters (OPEs) and 26 polyfluoralkyl substances (PFASs) contained in dust. All the analytes were determined in HPLC/MS-MS, and OPEs were also analyzed in GC/MS, and the results were compared. The study was conducted through the investigation of the Standard Reference Material SRM 2585 of the National Institute of Standard and Technology (NIST). The results were compared with the available reference mass fraction reported in the NIST certificate. The mass fraction obtained for the other OPEs and PFASs was compared to available data in the literature. After verifying the reliability of the results, the method was applied to environmental samples of settled dust, collected in four workplaces, where OPE and PFAS content is expected to be higher than in house dust: a mechanical workshop, an electronic repair center, a disassembly site, and a shredding site of two electronic waste recycling plants. By analyzing both PFASs and OPEs in the same samples, the present work demonstrated that the selected working places were more polluted in OPEs than houses; on the contrary, PFAS content in house dust proved to be more than ten times higher than that in workplaces. Additional research is necessary to confirm these data. Nevertheless, because this preliminary study showed not negligible concentrations of OPEs in some workplaces and of PFASs in houses, their monitoring should be extended to other domestic and selected working sites.

A review of organophosphate esters in soil: Implications for the potential source, transfer, and transformation mechanism.

Organophosphate esters (OPEs) are widely used around the world as flame retardants and plasticizers with a growing production in the last 15 years due to the phase-out of polybrominated diphenyl ethers. Multiple papers reported the occurrences of OPEs in various environmental matrices and elevated concentrations of OPEs (0.1-10,000ng/g dry weight) were documented in different types of soils which were regarded as both the "sink" and "source" of OPEs. In this study, the source, transfer, and transformation mechanisms of OPEs are systematically reviewed from the perspective of the soil environment. The wet/dry deposition, air-soil exchange, sewage irrigation, sludge application, and indirect oxidization of organophosphate antioxidants are the possible sources of OPEs in soil. Meanwhile, the OPEs in the soil environment may also migrate into other environmental media via plant uptake, air-soil exchange, desorption, and infiltration to cause relevant ecological risk, which depends much on the chemical properties of these compounds. The trimethylphenyl phosphate (TMPP) (mixture of isomers) and triphenyl phosphate (TPHP), which have strong hydrophobicity, pose a higher ecological risk for the soil environment than other OPEs. Further, the hydrolysis, indirect photolysis, and biodegradation of OPEs in the soil environment may be affected by the soil pH, organic acid, dissolved metals and metal oxides, active oxygen species, and microorganisms significantly. Besides that, the human exposure risks of OPEs from the soil are limited compared to those via indoor dust and food ingestion pathways. Finally, this study identifies the knowledge gaps and generated the future perspectives of the OPEs in soil.

Occupational Exposure of Canadian Nail Salon Workers to Plasticizers Including Phthalates and Organophosphate Esters.

Personal exposure of nail salon workers to 10 phthalates and 19 organophosphate esters (OPEs) was assessed in 18 nail salons in Toronto, Canada. Active air samplers (n = 60) and silicone passive samplers, including brooches (n = 58) and wristbands (n = 60), were worn by 45 nail salon workers for ∼8 working hours. Diethyl phthalate (median = 471 ng m-3) and diisobutyl phthalate (337 ng m-3) were highest in active air samplers. Most abundant OPEs in active air samplers were tris(2-chloroisopropyl)phosphate or TCIPP (303 ng m-3) and tris(2-chloroethyl)phosphate or TCEP (139 ng m-3), which are used as flame retardants but have not been reported for use in personal care products or nail salon accessories. Air concentrations of phthalates and OPEs were not associated with the number of services performed during each worker's shift. Within a single work shift, a combined total of 16 (55%) phthalates and OPEs were detected on passive silicone brooches; 19 (66%) were detected on wristbands. Levels of tris(2-chloroisopropyl)phosphate, tris(1,3-dichloro-2-propyl)phosphate or TDCIPP, and triphenyl phosphate or TPhP wristbands were significantly higher than those worn by e-waste workers. Significant correlations (p < 0.05) were found between the levels of some phthalates and OPEs in silicone brooches and wristbands versus those in active air samplers. Stronger correlations were observed between active air samplers versus brooches than wristbands. Sampler characteristics, personal characteristics, and chemical emission sources are the three main factors proposed to influence the use of passive samplers for measuring semi-volatile organic compound exposure.

Organophosphate esters in surface waters of Shandong Peninsula in eastern China: Levels, profile, source, spatial distribution, and partitioning

Organophosphate ester (OPE) levels, profiles, sources, spatial distribution, and partitioning were firstly studied in the rivers of the Shandong Peninsula. A total of 53 water samples and 45 sediment samples were collected from the rivers and the sewage treatment plant in the peninsula to quantitate levels of 13 targeted OPEs. Total OPE concentrations ranged from 263 to 6676 ng L−1 in the water, and 39.3–360 ng g−1 in the sediment. TEP, TCPP, and TCEP together contributed more than 90% of total OPE content. TCEP and TCPP concentrations in the Xiaoqing River sediment were increased by approximately two and seven times from 2014 to 2019, respectively. Total OPE concentrations generally increased from upstream regions to the estuaries. The main OPE sources were municipal effluent in the Jiaozhou Bay (JZB) watershed and chemical industrial wastewater in the Laizhou Bay (LZB) watershed. TCPP, TEP, and TCEP were generally approaching equilibrium between sediment and overlying water, while TNBP, TIBP, and TBOEP effectively transferred from the overlying water to the sediment. The riverine OPE flux was 0.66 ton/year to JZB and 3.58 ton/year to the LZB. TCPP and TCEP in municipal effluent, and TEP in chemical industrial wastewater should be regulated to protect Shandong Peninsula waters.

Organophosphate esters in tree bark and human hair in Weifang and Yantai, Shandong Province, China: concentrations, profiles and sources

Organophosphate ester (OPE) concentrations and distributions in 15 tree bark and 59 human hair samples from Weifang and Yantai (Shandong Province, China) were determined. The total OPE concentrations in tree bark samples from Weifang and Yantai were 16.5 ng/g-78.5 ng/g and 9.34 ng/g-98.6 ng/g dry weight (dw), respectively. The total OPE concentrations in hair samples from Weifang and Yantai were 54.2 ng/g dw-8450 ng/g dw and 7.26 ng/g dw -13,900 ng/g dw, respectively. Chlorinated OPEs were dominant in the tree bark samples from both Weifang and Yantai. Tris(2-chloroethyl)phosphate (TCEP) was the dominant OPE in the hair samples from residents of Weifang and Yantai. Attention should be paid to human exposure to TCEP, which is carcinogenic. The OPE concentrations in human hair were highest for the &lt; 20 years age group. The OPE patterns between the two cities were similar for both tree bark and hair, but the OPE patterns in the tree bark and hair samples from the same place were significantly different. This indicates that the outdoor atmosphere may not be the main source of OPEs in human hair.

Human exposure assessment of organophosphate esters (OPEs) through dust ingestion and dermal absorption in Colombian cities

Concentrations of 19 organophosphate esters (OPEs) were determined in dust samples collected from house and car indoor microenvironments in three Colombian cities. ∑OPE concentrations ranged from 1.31 to 599 μg/g. Mean concentrations of dust homes were 82.6, 48.3, and 46.7 μg/g for Cartagena, Bogotá, and Medellín, respectively. The pollution inside cars was somewhat higher than in houses, with a mean value of 231 μg/g. Sixteen compounds were detected, being TPHP, DCP, TEP, and TCEP the most frequently detected. As for OPEs with higher levels in houses, we found (mean ± SD) 35.2 ± 37.1 μg/g for TDCIPP in Cartagena, 35.6 ± 80.2 μg/g for TPHP in Cartagena, 15.9 ± 31.4 μg/g for DCP in Cartagena, 35.7 ± 19.1 μg/g for TBOEP in Bogotá, 15.7 ± 14.8 μg/g for 4IPPDPP in Medellín, and 17.5 ± 22.9 μg/g for TCEP in Cartagena, while the highest OPE value found in cars was 176 ± 144 μg/g for TDCIPP. The estimated daily intake (EDI) of OPEs through dust ingestion ranged from 0.001 ng/kg bw/day for adults to 110 ng/kg bw/day for toddlers, while dermal absorption ranged from 0.02 ng/kg bw/day for adults to 42.7 ng/kg bw/day for infants. Overall, the EDIs of dust ingestion were three times greater than those of dust dermal absorption. The estimated EDIs were several orders of magnitude below the corresponding reference doses. However, the incremental lifetime cancer risk (ILCR) for TCEP ranged from 1.1 × 10-5 for infants in Bogotá to 4.3 × 10-4 for adults in Cartagena, while ILCR for TEHP ranged from 8.8 × 10-7 for infants in Bogotá to 1.1 × 10-5 for adults in Bogotá. These estimated ILCRs were higher than the safe limit value of 1 × 10-6 and showed that these populations are exposed to moderate cancer risk.

Distribution of organophosphate esters influenced by human activities and fluvial-tidal interactions in the Dong Nai River System, Vietnam

Limited information is known about organophosphate esters (OPEs) in sediments of the Dong Nai River System (DNRS) in Vietnam and the influences of complex hydro-sedimentary dynamics on their fate. In this study, 48 surface sediment samples were collected from the Dong Nai-Soai Rap River and its tributary Vam Co River for the determination of 11 target OPEs, together with grain size and total organic carbon (TOC). The total concentrations of OPEs were in the range of 39.4 ng/g dw–373 ng/g dw (mean: 128 ng/g dw), and tris(1-chloro-2-propyl) phosphate (TCPP) was the predominant one with an average contribution of 81%, followed by tri-n-butyl phosphate (TNBP), tris(2-ethylhexyl) phosphate (TEHP). The composition profiles of OPEs at different locations of the DNRS showed no significant differences (p > 0.05). In addition, the distribution of OPEs had been influenced by both human activities and the fluvial-tidal interactions. The highly frequent and various human activities in Ho Chi Minh City (HCMC) leaded to the highest total concentration of OPEs in the midstream site. Based on our dataset, TOC content and grain size of sediments had significant correlation with certain OPEs (p < 0.05), and sediments with higher TOC content and finer grain size in the DNRS were more likely to be deposited in the downstream reach, contributing to the estuary of the DNRS was identified as another hotspot with the second highest concentration of OPEs. Furthermore, the distribution of OPEs in the transects had distinct characteristics, which reflected the joint influence of the human activities and fluvial-tidal interaction as well. However, the mechanism of their influence needed further investigation.

High-Resolution Mass Spectrometry Screening of Emerging Organophosphate Esters (OPEs) in Wild Fish: Occurrence, Species-Specific Difference, and Tissue-Specific Distribution.

There is a dearth of information regarding the pollution status of emerging organophosphate esters (OPEs) in wild fish. Here, we optimized and validated a quick, easy, cheap, effective, rugged, and safe (QuEChERS) pretreatment method, which was further applied for target, suspect, and nontarget screening of OPEs in n = 48 samples of wild fishes from Taihu Lake (eastern China). This integrated technique allows us to fully identify 20 OPEs, and 9 out of them are emerging OPEs detected in wild fish for the first time. Importantly, some of the emerging OPEs, i.e., tris(2,4-di-tert-butylphenyl) phosphate (TDtBPP), 4-tert-butylphenyl diphenyl phosphate (BPDP), and 2-isopropylphenyl diphenyl phosphate (IPDP), exhibited greater or at least comparable contamination levels as compared to traditional ones. There were no statistically significant interspecies (n = 6) differences regarding OPE concentrations. However, we observed significant differences on OPE concentrations among different tissues of silver carp (Hypophthalmichthys molitrix), for which the intestine has the highest OPE mean concentration (46.5 ng/g wet weight (ww)), followed by the liver (20.1 ng/g ww) ≈ brain (20.0 ng/g ww) > gill (14.8 ng/g ww) > muscle (11.4 ng/g ww). An interesting exception is IPDP, which presents an unexpectedly high concentration in the brain (0.510 ng/g ww). Collectively, this study expands our understanding of OPE contamination in wild fish and clearly shows that emerging TDtBPP, IPDP, and BPDP could play an equally important role as traditional OPEs in contribution of OPE pollution in wild fish samples.

Occurrence and risk assessment of organophosphate esters and bisphenols in San Francisco Bay, California, USA

Organophosphate esters (OPEs) and bisphenols are two classes of industrial chemicals that are ubiquitously detected in environmental matrices due to high global production and widespread use, particularly in the manufacture of plastic products. In 2017, water samples collected throughout the highly urbanized San Francisco Bay were analyzed for 22 OPEs and 16 bisphenols using liquid chromatography-electrospray ionization-Q Trap-mass spectrometry. Fifteen of the 22 OPEs were detected, with highest median concentrations in the order TCPP (42 ng/L) > TPhP (9.5 ng/L) > TBOEP (7.6 ng/L) > TnBP (7.5 ng/L) > TEP (6.7 ng/L) > TDCIPP (6.2 ng/L). In contrast, only two of 16 bisphenols, BPA and BPS, were quantified, with concentrations ranging from <0.7–35 ng/L and <1–120 ng/L, respectively. BPA and a few OPEs (EHDPP and TEHP) were primarily present in the particulate phase, while BPS and all other observed OPEs were predominantly found in the dissolved phase. Pairwise correlation analysis revealed several strong, positive correlations among OPEs, and few weak, negative correlations between OPEs and BPA, suggesting differences between the two classes with respect to their sources, pathways, and/or fate in the environment. Concentrations of OPEs and bisphenols observed in this study were generally consistent with reported concentrations in other estuarine and marine settings globally. TDCIPP exceeded existing predicted no-effect concentrations (PNECs) at some sites, and six other compounds (TCrP, IDDPP, EHDPP, TPhP, TBOEP, and BPA) were observed at levels approaching individual compound PNECs (not considering mixture effects), indicating potential risks to Bay biota. These results emphasize the need to control releases of these contaminants in order to protect the ecosystem. Periodic monitoring can be used to maintain vigilance in the face of potential regrettable substitutions.

Semi-volatile organic compounds in fine particulate matter on a tropical island in the South China Sea

Measurements of hazardous semi-volatile organic compounds (SVOCs) in remote tropical regions are rare. In this study, polycyclic aromatic compounds (PACs) [including polycyclic aromatic hydrocarbons (PAHs), nitrated PAHs (NPAHs), and oxygenated PAHs (OPAHs)], organophosphate esters (OPEs), and phthalic acid esters (PAEs) were measured in fine particulate matter (PM2.5) at Yongxing Island in the South China Sea (SCS). The concentrations of PACs (median = 53.5 pg/m3) were substantially low compared with previous measurements. The concentration weighted trajectory (CWT) model showed that the eastern and southern China was the main source region of PAC, occurring largely during the northeast (NE) monsoon. The PM2.5 showed remarkably high concentrations of OPEs (median = 3231 pg/m3) and moderate concentrations of PAEs (13,013 pg/m3). Some Southeast Asian countries were largely responsible for their higher concentrations, driven by the tropical SCS monsoons. We found significant atmospheric loss of the SVOCs, which is an explanation for the low concentrations of PACs. Enhanced formation of N/OPAHs originated from tropical regions was also observed. The positive matrix factorization model was applied to apportion the SVOC sources. The results, as well as correlation analyses of the SVOC concentrations, further indicate insignificant local sources and enhanced atmospheric reactions on this island.

Partial dust removal in vehicles does not mitigate human exposure to organophosphate esters

Organophosphate esters (OPEs) have been detected within car interior dust, suggesting that the indoor microenvironment of vehicles may represent a potential route of human exposure to OPEs. We recently showed that people with longer commutes are exposed to higher concentrations of tris(1,3-dichloro-2-isopropyl)phosphate (TDCIPP) – a widely used OPE – and other studies have suggested that dust removal may lead to lower exposure to chemicals. Therefore, the overall objective of this study was to determine if a decrease in interior car dust results in mitigation of personal OPE exposure. Participants (N = 49) were asked to wear silicone wristbands, and a subset of them wiped interior parts at the front of their vehicles prior to one study week (N = 25) or both study weeks (N = 11). There were no significant differences in total OPE concentrations (77.79–13,660 ng/g) nor individual OPE concentrations (0.04–4852.81 ng/g) across the different wiping groups nor in relation to participant residence ZIP codes and AC/Heater usage. These findings suggest that higher exposure to TDCIPP for participants with longer commutes may be independent of dust located on interior parts at the front of the vehicle. Therefore, our study demonstrates that there is a need for research on the potential contribution of other sources of TDCIPP exposure within car interiors.

Bioaccumulation and translocation of organophosphate esters in a Mangrove Nature Reserve from the Pearl River Estuary, South China

Little is known about the distribution and bioaccumulation of organophosphate esters (OPEs) in mangrove ecosystems. In this study, water, sediments, plants and animals were collected from Qi'ao Island Mangrove Nature Reserve to investigate the levels, bioaccumulation and biomagnification of OPEs. Concentrations of ΣOPEs in the mangrove plant Sonneratia apetala (an exotic species) were greater than those in Kandelia obovata (a native species). Translocation factors of OPEs in the two mangrove tree species were greater than 1, indicating that OPEs were mainly absorbed in aboveground tissues. Concentrations of OPEs in mangrove trees and animals were negatively correlated with their log Kow, suggesting that accumulation of OPEs in mangrove biota was influenced by hydrophobicity. A significant difference for concentrations of ΣOPEs was found among the eight mangrove animal species. Concentrations of ΣOPEs in mangrove animals were related with lipid contents, feeding habits and Kow of OPEs. Biota-sediment accumulation factor of OPEs was larger than 1, suggesting that bioaccumulation of OPEs occurred in mangrove animals. The targeted OPEs except isodecyl diphenyl phosphate were not biomagnified in mangrove animals. This study highlights bioaccumulation of OPEs in mangrove biota and suggests further concern about the ecological risk of OPEs to mangrove biota.

Occurrence, potential sources and risks of organophosphate esters in the high-elevation region, Tibet, China

Organophosphate esters (OPEs) are widely used flame retardants that are frequently released into the environment, causing potential harm to humans and ecosystems. Tibet is located on the Tibetan Plateau, known as the “roof of the world”, but the occurrence of OPEs in Tibet remains unclear. This is the first report of the occurrence, potential sources and risks of 12 OPEs in water, soil, sediment and snow from Xainza, a typical town at high-elevation in Tibet (average elevation = 4700 m). Ten OPEs were observed, with ∑OPE concentrations of 46.45–1744.73 ng/L in surface water, 29.74–73.85 ng/g in soil, and 13.30–32.23 ng/g in sediment. Moreover, the mean ∑OPE concentration in snow was 413.90 ng/L. Tris (2-chloroethyl) phosphate (TCEP) and tris (2-chloroisopropyl) phosphate (TCPP) were the main OPEs in surface water and snow, while 2-ethylhexyl diphenyl phosphate (EHDPP) was dominant in soil and sediment. Local human activities and long-distance atmospheric transport may be the main sources of OPEs in Xainza. The assessment of ecological risk indicated that EHDPP in soil poses potential risk. The occurrence of OPEs in Xainza showed that more attention should be paid to persistent organic pollutants in high-elevation regions.

Maternal urinary OPE metabolite concentrations and blood pressure during pregnancy: The HOME study

BackgroundFew studies have examined the association between maternal exposure to organophosphate esters (OPEs) and systolic/diastolic blood pressure (SBP/DBP) during pregnancy. MethodsWe analyzed data from 346 women with a singleton live birth in the HOME Study, a prospective birth cohort in Cincinnati, Ohio, USA. We quantified four OPE metabolites in maternal spot urine samples collected at 16 and 26 weeks pregnancy, standardized by specific gravity. We calculated intraclass correlation coefficients (ICCs). We extracted the first two recorded BP measurements (<20 weeks), the two highest recorded BP measurements (≥20 weeks), and diagnoses of hypertensive disorders of pregnancy (HDP) via chart review. Women with two BP measurements ≥140/90 mmHg or HDP noted in the chart at ≥20 weeks pregnancy were defined as HDP cases. We used linear mixed models and modified Poisson regression with covariate adjustment to estimate associations between OPE concentrations as continuous variables or in tertiles with maternal BP and HDP. ResultsICCs of OPEs were 0.17–0.45. Diphenyl phosphate (DPHP) had the highest geometric mean concentration among OPE metabolites. Increasing the average bis(2-chloroethyl) phosphate (BCEP) concentrations were positively associated with two highest recorded DBP ≥20 weeks pregnancy. Compared with women in the 1st DPHP tertile, women in the 3rd tertile at 16 weeks pregnancy had 1.72 mmHg (95% CI: -0.01, 3.46) higher DBP <20 weeks pregnancy, and women in the 3rd tertile of the average DPHP concentrations had 2.25 mmHg (95% CI: 0.25, 4.25) higher DBP ≥20 weeks pregnancy. 33 women (9.5%) were identified with HDP. Di-n-butyl phosphate (DNBP) concentrations at 16 weeks were positively associated with HDP, with borderline significance (RR = 2.98, 95% CI 0.97–9.15). Other OPE metabolites were not significantly associated with HDP. ConclusionMaternal urinary BCEP and DPHP concentrations were associated with increased BP during pregnancy. Maternal urinary DNBP concentrations were associated with HDP, with borderline significance.

Organophosphate ester plasticizers in edible fish from the Mediterranean Sea: Marine pollution and human exposure

Concentrations of organophosphate esters (OPEs) plasticizers were analysed in the present study. Fifty-five fish samples belonging to three highly commercial species, European sardine (Sardina pilchardus), European anchovy (Engraulis encrasicolus), and European hake (Merluccius merluccius), were taken from the Western Mediterranean Sea. OPEs were detected in all individuals, except for two hake samples, with concentrations between 0.38 and 73.4 ng/g wet weight (ww). Sardines presented the highest mean value with 20.5 ± 20.1 ng/g ww, followed by anchovies with 14.1 ± 8.91 ng/g ww and hake with 2.48 ± 1.76 ng/g ww. The lowest OPE concentrations found in hake, which is a partial predator of anchovy and sardine, and the higher δ15N values (as a proxy of trophic position), may indicate the absence of OPEs biomagnification. Eleven out of thirteen tested OPEs compounds were detected, being diphenyl cresyl phosphate (DCP) one of the most frequently detected in all the species. The highest concentration values were obtained for tris(1,3-dichloro-2-propyl) phosphate (TDClPP), trihexyl phosphate (THP), and tris(2-butoxyethyl) phosphate (TBOEP), for sardines, anchovies, and hakes, respectively. The human health risk associated with the consumption of these fish species showing that their individual consumption would not pose a considerable threat to public health regarding OPE intake.

A global systematic review on the concentration of organophosphate esters in water resources: Meta-analysis, and probabilistic risk assessment

Organophosphate esters (OPEs) are used as additives in various industries. They do not chemically bond with the polymeric structure of materials, so they can stay for a long time and have a very adverse effect on the environment. To analyze the development of the prevalence and concentration of OPEs such as TCEP, TCPP, TDCP, TnBP, TPHP, TBOEP, TEHP, TMP, TCIPP, TDCIPP, TMPP, and TDBPP in water resources, a search between January 01, 2000, to April 08, 2021, was followed by a systematic review and meta-analysis. Among of the 888 articles scanned in the identity step, 58 articles containing 2676 samples, 10 countries, and 4 water types were included in the meta-analysis study. Among all studied OPEs, the concentration of TcrP, TCPP, TDCPP, and TnBP were at the top in water resources, with values >715 μg L−1 and lowest average concentrations were obtained for TDBPP and TpeP with values <0.0004 μg L−1. The most polluted area in terms of the concentration of OPEs in water resources was China. Besides, data analysis showed that there only was carcinogenic risk for China. A Monte-Carlo simulation indicated that although these obtained averages are in the same order of magnitude as the acceptable limit, for both adults and children, 95% of the population is at risk.

Atmospheric deposition, seasonal variation, and long-range transport of organophosphate esters on Yongxing Island, South China Sea

The South China Sea (SCS), surrounded by developing countries/regions with a huge consumption of flame retardants, is generally contaminated by organophosphate esters (OPEs). However, studies on the occurrence, deposition and long-range atmospheric transport (LRAT) process over the SCS of OPEs compounds are still limited. In this work, 10 OPEs were measured in 100 atmospheric samples collected from Yongxing Island (YXI) in the SCS. The total OPEs concentrations ranged from 1508 to 1968 pg/m3 with 28.6–1416.9 pg/m3 in gas and 95.2–1066.2 pg/m3 in particle partition. The three chlorinated OPEs are present at higher concentrations than the other seven non-chlorinated OPEs. Most OPEs had clear seasonal variations that followed the order: spring>summer≈winter>autumn except for tri-isobutyl phosphate (TIBP) and tris-(2-ethylhexyl) phosphate (TEHP). The particle-bound fraction of the total OPEs had little seasonal variations with a mean value of 0.35. Comparing J-P model and Koa model, it was found that the gas/particle partition in the study area was in non-equilibrium condition. LRAT, controlled by seasonal wind direction, was the predominated factor that led to the seasonal variations of OPEs on YXI. The average daily deposition flux of total OPEs was 13.0 ng/m2 with an annual total deposition of 15.06 g.